Evidence map›Paper›PMID 42187010›Full record

ArticleCancer medicine2026

Real-World Efficacy of Metronomic Chemotherapy in Advanced Breast Cancer Across Molecular Subtypes.

Hanxing Zhou, Linmin Chen, Qianyi Lu, Huailiang Wu, Kuikui Jiang, Fei Xu, Shusen Wang

Abstract read
In one paragraph

Article in Cancer medicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

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0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Hanxing ZhouState Key Laboratory of Oncology in South China, Collaborative Innovation Center for Cancer Medicine, Department of Medical Oncology, Sun Yat-Sen University Cancer Center, Guangzhou, Guangdong, China.
Linmin ChenState Key Laboratory of Oncology in South China, Collaborative Innovation Center for Cancer Medicine, Department of Medical Oncology, Sun Yat-Sen University Cancer Center, Guangzhou, Guangdong, China.
Qianyi LuState Key Laboratory of Oncology in South China, Collaborative Innovation Center for Cancer Medicine, Department of Medical Oncology, Sun Yat-Sen University Cancer Center, Guangzhou, Guangdong, China.
Huailiang WuState Key Laboratory of Oncology in South China, Collaborative Innovation Center for Cancer Medicine, Department of Medical Oncology, Sun Yat-Sen University Cancer Center, Guangzhou, Guangdong, China.ORCID https://orcid.org/0000-0002-2040-3945
Kuikui JiangState Key Laboratory of Oncology in South China, Collaborative Innovation Center for Cancer Medicine, Department of Medical Oncology, Sun Yat-Sen University Cancer Center, Guangzhou, Guangdong, China.ORCID https://orcid.org/0000-0003-4498-8404
Fei XuState Key Laboratory of Oncology in South China, Collaborative Innovation Center for Cancer Medicine, Department of Medical Oncology, Sun Yat-Sen University Cancer Center, Guangzhou, Guangdong, China.
Shusen WangState Key Laboratory of Oncology in South China, Collaborative Innovation Center for Cancer Medicine, Department of Medical Oncology, Sun Yat-Sen University Cancer Center, Guangzhou, Guangdong, China.ORCID https://orcid.org/0000-0003-0139-5780

Funding

Beijing Xisike Clinical Oncology Research Foundation Y-Gilead2024-PT-029he Sun Yat-sen University Clinical Research 5010 Program 2017011the National Health Commission of the People's Republic of China and the National Science and Technology Major Project for the Prevention and Treatment of Cancer, Cardiovascular and Cerebrovascular Diseases, Respiratory and Metabolic Diseases No. 2023ZD0502303the National Natural Science Foundation of China 82573358
6 · The paper itself

Abstract

objectiveMetronomic chemotherapy (mCHT) is widely used in the treatment of breast cancer due to its low toxicity and convenience. However, there remain real-world studies with satisfactory samples focusing on mCHT in advanced breast cancer.

methodsEnrolled patients were assigned into capecitabine-based (X-based) group and other mCHT group. Data on baseline characteristics, treatment regimens, and outcomes were extracted from medical records. Kaplan-Meier estimates of progression-free survival (PFS) and overall survival (OS) were analyzed.

resultsTotally, 597 patients were included with median follow-up time of 35.9 months. The median PFS for X-base group was significantly higher than that in other mCHT group (8.9 vs. 5.9 months, p = 0.004). As salvage therapy, the X-based group showed significantly higher PFS and OS than the other mCHT group in patients with HR + HER2- breast cancer (p < 0.001 and p = 0.011), especially in those combined with endocrine therapy (ET). Multivariate Cox analysis revealed that additional ET could reduce the disease progression and death risks (HR = 0.60, 95% CI: 0.44-0.81; HR = 0.66, 95% CI: 0.47-0.93). In HER2+ and TNBC populations, the median PFS was higher when used as maintenance therapy compared to salvage therapy (16.0 vs. 7.0 months, p < 0.001; 11.0 vs. 5.0 months, p = 0.030).

conclusionAs salvage therapy, mCHT demonstrated significant efficacy advantages in the X-based group compared to the other mCHT group in patients with HR + HER2- breast cancer, especially in those combined with ET. For HER2+ and TNBC patients, mCHT is recommended as maintenance therapy.

Indexed as

Antineoplastic Combined Chemotherapy ProtocolsBreast NeoplasmsCapecitabineAdministration, MetronomicAdultAntimetabolites, AntineoplasticErb-b2 Receptor Tyrosine KinasesFemaleFollow-Up StudiesHumansKaplan-Meier EstimateMaintenance ChemotherapyMiddle AgedNeoplasm StagingPrognosisProgression-Free SurvivalAntimetabolites, AntineoplasticCapecitabineERBB2 protein, humanErb-b2 Receptor Tyrosine Kinasesadvanced breast cancercapecitabinemaintenancemetronomic chemotherapysalvage

Identifiers

PMID42187010
PMCPMC13240560

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.